Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Barbara Gianesin"'
Autor:
Valeria Maria Pinto, Barbara Gianesin, Salvatore Sardo, Filippo Mazzi, Giammarco Baiardi, Sofia Menotti, Fabio Piras, Sabrina Quintino, Giacomo Robello, Francesca Mattioli, Gabriele Finco, Gian Luca Forni, Lucia De Franceschi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-5 (2024)
Abstract Pain is an hallmark of sickle-cell-related acute clinical manifestations as part of acute vaso-occlusive crisis (VOC). In SCD pain has different origins such as vascular or neuropathic pain, which requires multimodal analgesia. This is based
Externí odkaz:
https://doaj.org/article/7d0cb2daaaaf4f75969177fdc5fd3dc6
Autor:
Veronica Bordoni, Maddalena Casale, Valeria Maria Pinto, Rita Carsetti, Barbara Gianesin, Maria Rita Gamberini, Leila Mazdai, Susanna Barella, Anna Rita Denotti, Francesca Colavita, Silverio Perrotta, Aurelio Maggio, Lorella Pitrolo, Sabrina Quintino, Marco Caminati, Filippo Mazzi, Jacopo Ceolan, Lucia De Franceschi, Gian Luca Forni, Franco Locatelli, Chiara Agrati
Publikováno v:
HemaSphere, Vol 7, p e98163b7 (2023)
Externí odkaz:
https://doaj.org/article/61f3b3097b73470598f72a91beb56bfe
Autor:
Valeria Maria Pinto, Barbara Gianesin, Salvatore Sardo, Filippo Mazzi, Giammarco Baiardi, Sofia Menotti, Fabio Piras, Gabriele Finco, Gian Luca Forni, Lucia De Franceschi
Publikováno v:
HemaSphere, Vol 7, p e2003822 (2023)
Externí odkaz:
https://doaj.org/article/d6b333fde8a94cf38bd5dd1bfe3a40c9
Autor:
Valeria Maria Pinto, Lorenzo Bacigalupo, Barbara Gianesin, Andrea Cazzato, Sabrina Quintino, Gian Luca Forni
Publikováno v:
HemaSphere, Vol 7, p e9400165 (2023)
Externí odkaz:
https://doaj.org/article/3daac3a9862748f988c028bf7dfd2b48
Autor:
Valeria Maria Pinto, Barbara Gianesin, Frédéric B. Piel, Filomena Longo, Paolo Rigano, Alessandra Quota, Vincenzo Spadola, Giovanna Graziadei, Filippo Mazzi, Maria Domenica Cappellini, Aurelio Maggio, Antonio Piga, Lucia De Franceschi, Gian Luca Forni
Publikováno v:
Haematologica, Vol 108, Iss 4 (2022)
Externí odkaz:
https://doaj.org/article/dceb93b8ce9d46abba2232e2a4b8c515
Autor:
Valeria Maria Pinto, Lucia De Franceschi, Barbara Gianesin, Antonia Gigante, Giovanna Graziadei, Letizia Lombardini, Giovanni Palazzi, Alessandra Quota, Rodolfo Russo, Laura Sainati, Donatella Venturelli, Gian Luca Forni, Raffaella Origa
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 10, p 3441 (2023)
The number of individuals with the sickle cell trait exceeds 300 million worldwide, making sickle cell disease one of the most common monogenetic diseases globally. Because of the high frequency of sickle cell disease, reproductive counseling is of c
Externí odkaz:
https://doaj.org/article/5dcc7efdc7a442cd83955ee349fc5ffb
Autor:
Giorgio Derchi, Khaled M. Musallam, Valeria Maria Pinto, Giovanna Graziadei, Marianna Giuditta, Susanna Barella, Raffaella Origa, Gavino Casu, Annamaria Pasanisi, Filomena Longo, Maddalena Casale, Roberta Miceli, Pierluigi Merella, Barbara Gianesin, Pietro Ameri, Immacolata Tartaglione, Silverio Perrotta, Antonio Piga, Maria Domenica Cappellini, Gian Luca Forni
Publikováno v:
Haematologica, Vol 107, Iss 7 (2022)
Externí odkaz:
https://doaj.org/article/cc1bf23e68984769acbf9393f0a002ab
Autor:
Giovanna Graziadei, Lucia De Franceschi, Laura Sainati, Donatella Venturelli, Nicoletta Masera, Piero Bonomo, Aurora Vassanelli, Maddalena Casale, Gianluca Lodi, Vincenzo Voi, Paolo Rigano, Valeria Maria Pinto, Alessandra Quota, Lucia D. Notarangelo, Giovanna Russo, Massimo Allò, Rosamaria Rosso, Domenico D'Ascola, Elena Facchini, Silvia Macchi, Francesco Arcioni, Federico Bonetti, Enza Rossi, Antonella Sau, Saveria Campisi, Gloria Colarusso, Fiorina Giona, Roberto Lisi, Paola Giordano, Gianluca Boscarol, Aldo Filosa, Sarah Marktel, Paola Maroni, Mauro Murgia, Raffaella Origa, Filomena Longo, Marta Bortolotti, Raffaella Colombatti, Rosario Di Maggio, Raffaella Mariani, Alberto Piperno, Paola Corti, Carmelo Fidone, Giovanni Palazzi, Luca Badalamenti, Barbara Gianesin, Frédéric B. Piel, Gian Luca Forni
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Sickle cell disease (SCD) is a worldwide distributed hereditary red cell disorder characterized by recurrent acute vaso-occlusive crises (VOCs and anemia). Gold standard treatments are hydroxycarbamide (HC) and/or different red blood cell (RBC) trans
Externí odkaz:
https://doaj.org/article/398e4c9f5e034cb4a3d5f9a863a7b433
Autor:
Nicola Romano, Giammarco Baiardi, Valeria Maria Pinto, Sabrina Quintino, Barbara Gianesin, Riccardo Sasso, Andrea Diociasi, Francesca Mattioli, Roberta Marchese, Giovanni Abbruzzese, Antonio Castaldi, Gian Luca Forni
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 15, p 4524 (2022)
Neurodegeneration with brain iron accumulation (NBIA) comprises various rare clinical entities with brain iron overload as a common feature. Magnetic resonance imaging (MRI) allows diagnosis of this condition, and genetic molecular testing can confir
Externí odkaz:
https://doaj.org/article/eef2e73b533f42fc957f730697a72ee0
Autor:
Raffaella Origa, Monia Cinus, Maria Paola Pilia, Barbara Gianesin, Antonietta Zappu, Valeria Orecchia, Maria Grazia Clemente, Carla Pitturru, Anna Rita Denotti, Francesco Corongiu, Simona Piras, Susanna Barella
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 7, p 2010 (2022)
The aim of this study is the evaluation of the safety and the efficacy of long-term combination therapy deferasirox plus desferrioxamine and deferasirox plus deferiprone in a large group of transfusion-dependent thalassemia patients with high values
Externí odkaz:
https://doaj.org/article/ffbfed30348345fe871bd21578e3e37f